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Thermodynamic Stability of Fenclorim and Clopyralid

The present work reports an experimental thermodynamic study of two nitrogen heterocyclic organic compounds, fenclorim and clopyralid, that have been used as herbicides. The sublimation vapor pressures of fenclorim (4,6-dichloro-2-phenylpyrimidine) and of clopyralid (3,6-dichloro-2-pyridinecarboxyli...

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Autores principales: Almeida, Ana R. R. P., Pinheiro, Bruno D. A., Lobo Ferreira, Ana I. M. C., Monte, Manuel J. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8746602/
https://www.ncbi.nlm.nih.gov/pubmed/35011279
http://dx.doi.org/10.3390/molecules27010039
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author Almeida, Ana R. R. P.
Pinheiro, Bruno D. A.
Lobo Ferreira, Ana I. M. C.
Monte, Manuel J. S.
author_facet Almeida, Ana R. R. P.
Pinheiro, Bruno D. A.
Lobo Ferreira, Ana I. M. C.
Monte, Manuel J. S.
author_sort Almeida, Ana R. R. P.
collection PubMed
description The present work reports an experimental thermodynamic study of two nitrogen heterocyclic organic compounds, fenclorim and clopyralid, that have been used as herbicides. The sublimation vapor pressures of fenclorim (4,6-dichloro-2-phenylpyrimidine) and of clopyralid (3,6-dichloro-2-pyridinecarboxylic acid) were measured, at different temperatures, using a Knudsen mass-loss effusion technique. The vapor pressures of both crystalline and liquid (including supercooled liquid) phases of fenclorim were also determined using a static method based on capacitance diaphragm manometers. The experimental results enabled accurate determination of the standard molar enthalpies, entropies and Gibbs energies of sublimation for both compounds and of vaporization for fenclorim, allowing a phase diagram representation of the (p,T) results, in the neighborhood of the triple point of this compound. The temperatures and molar enthalpies of fusion of the two compounds studied were determined using differential scanning calorimetry. The standard isobaric molar heat capacities of the two crystalline compounds were determined at 298.15 K, using drop calorimetry. The gas phase thermodynamic properties of the two compounds were estimated through ab initio calculations, at the G3(MP2)//B3LYP level, and their thermodynamic stability was evaluated in the gaseous and crystalline phases, considering the calculated values of the standard Gibbs energies of formation, at 298.15 K. All these data, together with other physical and chemical properties, will be useful to predict the mobility and environmental distribution of these two compounds.
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spelling pubmed-87466022022-01-11 Thermodynamic Stability of Fenclorim and Clopyralid Almeida, Ana R. R. P. Pinheiro, Bruno D. A. Lobo Ferreira, Ana I. M. C. Monte, Manuel J. S. Molecules Article The present work reports an experimental thermodynamic study of two nitrogen heterocyclic organic compounds, fenclorim and clopyralid, that have been used as herbicides. The sublimation vapor pressures of fenclorim (4,6-dichloro-2-phenylpyrimidine) and of clopyralid (3,6-dichloro-2-pyridinecarboxylic acid) were measured, at different temperatures, using a Knudsen mass-loss effusion technique. The vapor pressures of both crystalline and liquid (including supercooled liquid) phases of fenclorim were also determined using a static method based on capacitance diaphragm manometers. The experimental results enabled accurate determination of the standard molar enthalpies, entropies and Gibbs energies of sublimation for both compounds and of vaporization for fenclorim, allowing a phase diagram representation of the (p,T) results, in the neighborhood of the triple point of this compound. The temperatures and molar enthalpies of fusion of the two compounds studied were determined using differential scanning calorimetry. The standard isobaric molar heat capacities of the two crystalline compounds were determined at 298.15 K, using drop calorimetry. The gas phase thermodynamic properties of the two compounds were estimated through ab initio calculations, at the G3(MP2)//B3LYP level, and their thermodynamic stability was evaluated in the gaseous and crystalline phases, considering the calculated values of the standard Gibbs energies of formation, at 298.15 K. All these data, together with other physical and chemical properties, will be useful to predict the mobility and environmental distribution of these two compounds. MDPI 2021-12-22 /pmc/articles/PMC8746602/ /pubmed/35011279 http://dx.doi.org/10.3390/molecules27010039 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Almeida, Ana R. R. P.
Pinheiro, Bruno D. A.
Lobo Ferreira, Ana I. M. C.
Monte, Manuel J. S.
Thermodynamic Stability of Fenclorim and Clopyralid
title Thermodynamic Stability of Fenclorim and Clopyralid
title_full Thermodynamic Stability of Fenclorim and Clopyralid
title_fullStr Thermodynamic Stability of Fenclorim and Clopyralid
title_full_unstemmed Thermodynamic Stability of Fenclorim and Clopyralid
title_short Thermodynamic Stability of Fenclorim and Clopyralid
title_sort thermodynamic stability of fenclorim and clopyralid
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8746602/
https://www.ncbi.nlm.nih.gov/pubmed/35011279
http://dx.doi.org/10.3390/molecules27010039
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